Publications by authors named "Sarah Helfmann"

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A mutation in CABP2, expressed in cochlear hair cells, causes autosomal-recessive hearing impairment.
Isabelle Schrauwen, Sarah Helfmann, Akira Inagaki, Friederike Predoehl, Mohammad Amin Tabatabaiefar

Am J Hum Genet· October 2012

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The crystal structure of the C₂A domain of otoferlin reveals an unconventional top loop region.
Sarah Helfmann, Piotr Neumann, Kai Tittmann, Tobias Moser, Ralf Ficner

J Mol Biol· February 2011

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Structure of GlnK1, a signalling protein from Archaeoglobus fulgidus.
Claudia Litz, Sarah Helfmann, Stefan Gerhardt, Susana L A Andrade

Acta Crystallogr Sect F Struct Biol Cryst Commun· February 2011

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Cooperative binding of MgATP and MgADP in the trimeric P(II) protein GlnK2 from Archaeoglobus fulgidus.
Sarah Helfmann, Wei Lü, Claudia Litz, Susana L A Andrade

J Mol Biol· September 2010

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